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PE20210548A1 - AMINO-FLUOROPIPERIDINE DERIVATIVE AS A KINASE INHIBITOR - Google Patents

AMINO-FLUOROPIPERIDINE DERIVATIVE AS A KINASE INHIBITOR

Info

Publication number
PE20210548A1
PE20210548A1 PE2020000773A PE2020000773A PE20210548A1 PE 20210548 A1 PE20210548 A1 PE 20210548A1 PE 2020000773 A PE2020000773 A PE 2020000773A PE 2020000773 A PE2020000773 A PE 2020000773A PE 20210548 A1 PE20210548 A1 PE 20210548A1
Authority
PE
Peru
Prior art keywords
amino
kinase inhibitor
fluoropiperidine
derivative
fluoropiperidine derivative
Prior art date
Application number
PE2020000773A
Other languages
Spanish (es)
Inventor
In Woo Kim
Nam Youn Kim
Seung Hwarn Jeong
Jun Hee Lee
Original Assignee
Dae Woong Pharma
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Dae Woong Pharma filed Critical Dae Woong Pharma
Publication of PE20210548A1 publication Critical patent/PE20210548A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

La presente invencion se refiere a un compuesto representado por la Formula 1 donde R1 es C1-5 alquil, halogeno, ciano; X es N-R2, O, S; R2 es C1-5 alquil, C1-5 haloalquil, C3-6 cicloalquil. El compuesto segun la presente invencion puede usarse de manera util para la prevencion o el tratamiento de enfermedades que estan asociadas con acciones inhibidoras de quinasas.The present invention relates to a compound represented by Formula 1 where R1 is C1-5 alkyl, halogen, cyano; X is N-R2, O, S; R2 is C1-5 alkyl, C1-5 haloalkyl, C3-6 cycloalkyl. The compound according to the present invention can be usefully used for the prevention or treatment of diseases which are associated with kinase inhibitory actions.

PE2020000773A 2017-12-28 2018-12-28 AMINO-FLUOROPIPERIDINE DERIVATIVE AS A KINASE INHIBITOR PE20210548A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
KR1020170183060A KR102577241B1 (en) 2017-12-28 2017-12-28 Amino-fluoropiperidine derivatives as kinase inhibitor
PCT/KR2018/016812 WO2019132560A1 (en) 2017-12-28 2018-12-28 Amino-fluoropiperidine derivative as kinase inhibitor

Publications (1)

Publication Number Publication Date
PE20210548A1 true PE20210548A1 (en) 2021-03-17

Family

ID=67063980

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2020000773A PE20210548A1 (en) 2017-12-28 2018-12-28 AMINO-FLUOROPIPERIDINE DERIVATIVE AS A KINASE INHIBITOR

Country Status (22)

Country Link
US (1) US11078206B2 (en)
EP (1) EP3733671B1 (en)
JP (1) JP7032535B2 (en)
KR (1) KR102577241B1 (en)
CN (1) CN111491934B (en)
AU (1) AU2018394995B2 (en)
BR (1) BR112020013164A2 (en)
CA (1) CA3084777C (en)
CL (1) CL2020001754A1 (en)
DO (1) DOP2020000109A (en)
EC (1) ECSP20035222A (en)
ES (1) ES2923682T3 (en)
MA (1) MA51429A (en)
MX (1) MX2020006708A (en)
MY (1) MY196186A (en)
PE (1) PE20210548A1 (en)
PH (1) PH12020551014A1 (en)
RU (1) RU2762637C1 (en)
SA (1) SA520412333B1 (en)
SG (1) SG11202004918XA (en)
TN (1) TN2020000125A1 (en)
WO (1) WO2019132560A1 (en)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2297344B1 (en) 2008-05-16 2018-03-14 Life Technologies Corporation Dual labeling methods for measuring cellular proliferation
MY200629A (en) 2017-08-01 2024-01-06 Theravance Biopharma R&D Ip Llc Pyrazolo and triazolo bicyclic compounds as jak kinase inhibitors
CN111527091B (en) 2017-12-28 2023-03-28 株式会社大熊制药 Oxy-fluoropiperidine derivatives as kinase inhibitors
KR102577242B1 (en) 2017-12-28 2023-09-11 주식회사 대웅제약 Amino-methylpiperidine derivatives as kinase inhibitor
CN113498352A (en) 2019-01-23 2021-10-12 施万生物制药研发Ip有限责任公司 Imidazo [1,5-A ] pyridines, 1,2, 4-triazolo [4,3-A ] pyridines and imidazo [1,5-A ] pyrazines as JAK inhibitors
KR102838154B1 (en) 2019-09-23 2025-07-28 피엠브이 파마슈티컬스 인코포레이티드 Methods and compounds for restoring mutant p53 function
US11697648B2 (en) 2019-11-26 2023-07-11 Theravance Biopharma R&D Ip, Llc Fused pyrimidine pyridinone compounds as JAK inhibitors
CN115244055B (en) * 2020-01-21 2024-09-03 江苏先声药业有限公司 Pyrimido five-membered ring derivatives and their applications
WO2021147952A1 (en) * 2020-01-21 2021-07-29 江苏先声药业有限公司 Pyrimidopyrrole compound
CN116096704A (en) 2020-06-24 2023-05-09 皮姆维制药公司 Combination therapy for the treatment of cancer
KR20230028371A (en) 2020-06-24 2023-02-28 피엠브이 파마슈티컬스 인코포레이티드 Companion Diagnostic Tool for Mutant P53 Reactivating Compounds
WO2022062601A1 (en) * 2020-09-22 2022-03-31 江苏先声药业有限公司 Pyrimidopyrrole compound
CN114315838B (en) * 2020-09-30 2024-09-03 江苏先声药业有限公司 Pyrimidopyrroles compounds
MX2024009235A (en) 2022-01-27 2024-08-06 Pmv Pharmaceuticals Inc Deuterated compounds for restoring mutant p53 function.

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7301023B2 (en) 2001-05-31 2007-11-27 Pfizer Inc. Chiral salt resolution
CN102159214A (en) 2008-07-16 2011-08-17 药品循环公司 Inhibitors of Bruton's tyrosine kinase for the treatment of solid tumors
EP2440559B1 (en) * 2009-05-05 2018-01-10 Dana-Farber Cancer Institute, Inc. Egfr inhibitors and methods of treating disorders
BR122014012788B1 (en) * 2010-06-23 2022-04-19 Hanmi Science Co., Ltd Fused pyrimidine derivatives, their uses, and pharmaceutical composition for inhibiting tyrosine kinase activity
CA2847540C (en) * 2011-09-22 2016-05-17 Pfizer Inc. Pyrrolopyrimidine and purine derivatives
PT2880035T (en) * 2012-08-06 2017-03-10 Acea Biosciences Inc Novel pyrrolopyrimidine compounds as inhibitors of protein kinases
WO2015039612A1 (en) 2013-09-18 2015-03-26 北京韩美药品有限公司 Compound inhibiting kinase activities of btk and/or jak3
ES2654051T3 (en) * 2013-12-05 2018-02-12 Pfizer Inc. Pyrrolo [2,3-d] pyrimidinyl, pyrrolo [2,3-b] pyrazinyl and pyrrolo [2,3-d] pyridinyl acrylamides
CN105732637B (en) * 2014-12-30 2020-04-21 广东东阳光药业有限公司 Heteroaromatic compounds and their application in medicine
WO2017106771A1 (en) * 2015-12-16 2017-06-22 Southern Research Institute Pyrrolopyrimidine compounds, use as inhibitors of the kinase lrrk2, and methods for preparation thereof
CN113135920A (en) * 2016-06-30 2021-07-20 株式会社大熊制药 Pyrazolopyrimidine derivatives as kinase inhibitors
KR102032418B1 (en) 2017-06-15 2019-10-16 한국화학연구원 Fused-pyrimidine derivatives, preparation method thereof, and pharmaceutical composition for use in preventing or treating Bruton's tyrosine kinase activity related diseases containing the same as an active ingredient

Also Published As

Publication number Publication date
KR102577241B1 (en) 2023-09-11
ECSP20035222A (en) 2020-07-31
NZ765159A (en) 2023-09-29
EP3733671B1 (en) 2022-06-29
EP3733671A4 (en) 2021-06-09
KR20190080540A (en) 2019-07-08
BR112020013164A2 (en) 2020-12-01
RU2762637C1 (en) 2021-12-21
CN111491934B (en) 2022-08-30
SG11202004918XA (en) 2020-06-29
MA51429A (en) 2021-04-07
PH12020551014A1 (en) 2021-08-16
MY196186A (en) 2023-03-21
CA3084777C (en) 2022-08-30
US11078206B2 (en) 2021-08-03
CL2020001754A1 (en) 2020-11-27
TN2020000125A1 (en) 2022-01-06
CN111491934A (en) 2020-08-04
CA3084777A1 (en) 2019-07-04
JP2021505644A (en) 2021-02-18
US20200299298A1 (en) 2020-09-24
AU2018394995A1 (en) 2020-06-25
AU2018394995B2 (en) 2021-05-13
SA520412333B1 (en) 2022-12-08
EP3733671A1 (en) 2020-11-04
DOP2020000109A (en) 2020-09-30
ES2923682T3 (en) 2022-09-29
WO2019132560A1 (en) 2019-07-04
MX2020006708A (en) 2020-08-20
JP7032535B2 (en) 2022-03-08

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